Canonical Allele Identifier: CA430310931
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189866161C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189001435C>A , CM000664.2:g.189001435C>A GRCh38
NC_000002.11:g.189866161C>A , CM000664.1:g.189866161C>A GRCh37
NC_000002.10:g.189574406C>A NCBI36
NG_007404.1:g.32063C>A , LRG_3:g.32063C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.2223C>A ENSP00000415346.2:p.Gly741=
ENST00000304636.9:c.2322C>A MANE Select ENSP00000304408.4:p.Gly774=
ENST00000304636.7:c.2322C>A ENSP00000304408.3:p.Gly774=
ENST00000317840.9:c.2322C>A ENSP00000315243.6:p.Gly774=
NM_000090.3:c.2322C>A , LRG_3t1:c.2322C>A NP_000081.1:p.Gly774=
NM_000090.4:c.2322C>A MANE Select NP_000081.2:p.Gly774=